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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1953 1
1955 1
1957 2
1958 1
1959 1
1961 1
1963 1
1964 2
1967 1
1968 1
1969 1
1971 4
1972 4
1973 3
1974 6
1975 5
1976 6
1977 8
1978 11
1979 9
1980 11
1981 13
1982 4
1983 6
1984 10
1985 9
1986 9
1987 7
1988 10
1989 2
1990 8
1991 5
1992 2
1993 8
1994 5
1995 4
1996 10
1997 6
1998 7
1999 20
2000 6
2001 12
2002 9
2003 12
2004 9
2005 8
2006 19
2007 19
2008 10
2009 10
2010 11
2011 16
2012 13
2013 13
2014 21
2015 18
2016 21
2017 22
2018 19
2019 15
2020 21
2021 19
2022 19
2023 22
2024 9

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560 results

Results by year

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Page 1
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice.
Sheppard SE, Bryant L, Wickramasekara RN, Vaccaro C, Robertson B, Hallgren J, Hulen J, Watson CJ, Faundes V, Duffourd Y, Lee P, Simon MC, de la Cruz X, Padilla N, Flores-Mendez M, Akizu N, Smiler J, Pellegrino Da Silva R, Li D, March M, Diaz-Rosado A, Peixoto de Barcelos I, Choa ZX, Lim CY, Dubourg C, Journel H, Demurger F, Mulhern M, Akman C, Lippa N, Andrews M, Baldridge D, Constantino J, van Haeringen A, Snoeck-Streef I, Chow P, Hing A, Graham JM Jr, Au M, Faivre L, Shen W, Mao R, Palumbos J, Viskochil D, Gahl W, Tifft C, Macnamara E, Hauser N, Miller R, Maffeo J, Afenjar A, Doummar D, Keren B, Arn P, Macklin-Mantia S, Meerschaut I, Callewaert B, Reis A, Zweier C, Brewer C, Saggar A, Smeland MF, Kumar A, Elmslie F, Deshpande C, Nizon M, Cogne B, van Ierland Y, Wilke M, van Slegtenhorst M, Koudijs S, Chen JY, Dredge D, Pier D, Wortmann S, Kamsteeg EJ, Koch J, Haynes D, Pollack L, Titheradge H, Ranguin K, Denommé-Pichon AS, Weber S, Pérez de la Fuente R, Sánchez Del Pozo J, Lezana Rosales JM, Joset P, Steindl K, Rauch A, Mei D, Mari F, Guerrini R, Lespinasse J, Tran Mau-Them F, Philippe C, Dauriat B, Raymond L, Moutton S, Cueto-González AM, Tan TY, Mignot C, Grotto S, Rena… See abstract for full author list ➔ Sheppard SE, et al. Among authors: raymond l. Sci Adv. 2023 Mar 10;9(10):eade1463. doi: 10.1126/sciadv.ade1463. Epub 2023 Mar 10. Sci Adv. 2023. PMID: 36897941 Free PMC article.
Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermia.
Kherraf ZE, Cazin C, Bouker A, Fourati Ben Mustapha S, Hennebicq S, Septier A, Coutton C, Raymond L, Nouchy M, Thierry-Mieg N, Zouari R, Arnoult C, Ray PF. Kherraf ZE, et al. Among authors: raymond l. Am J Hum Genet. 2022 Mar 3;109(3):508-517. doi: 10.1016/j.ajhg.2022.01.011. Epub 2022 Feb 15. Am J Hum Genet. 2022. PMID: 35172124 Free PMC article.
Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia.
Méreaux JL, Banneau G, Papin M, Coarelli G, Valter R, Raymond L, Kol B, Ariste O, Parodi L, Tissier L, Mairey M, Ait Said S, Gautier C, Guillaud-Bataille M; French SPATAX clinical network; Forlani S, de la Grange P, Brice A, Vazza G, Durr A, Leguern E, Stevanin G. Méreaux JL, et al. Among authors: raymond l. Brain. 2022 Apr 29;145(3):1029-1037. doi: 10.1093/brain/awab386. Brain. 2022. PMID: 34983064 Free article.
Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.
Novarino G, Fenstermaker AG, Zaki MS, Hofree M, Silhavy JL, Heiberg AD, Abdellateef M, Rosti B, Scott E, Mansour L, Masri A, Kayserili H, Al-Aama JY, Abdel-Salam GMH, Karminejad A, Kara M, Kara B, Bozorgmehri B, Ben-Omran T, Mojahedi F, El Din Mahmoud IG, Bouslam N, Bouhouche A, Benomar A, Hanein S, Raymond L, Forlani S, Mascaro M, Selim L, Shehata N, Al-Allawi N, Bindu PS, Azam M, Gunel M, Caglayan A, Bilguvar K, Tolun A, Issa MY, Schroth J, Spencer EG, Rosti RO, Akizu N, Vaux KK, Johansen A, Koh AA, Megahed H, Durr A, Brice A, Stevanin G, Gabriel SB, Ideker T, Gleeson JG. Novarino G, et al. Among authors: raymond l. Science. 2014 Jan 31;343(6170):506-511. doi: 10.1126/science.1247363. Science. 2014. PMID: 24482476 Free PMC article.
Employee Wellness Programs.
Raymond LW. Raymond LW. JAMA Intern Med. 2021 Feb 1;181(2):291. doi: 10.1001/jamainternmed.2020.5737. JAMA Intern Med. 2021. PMID: 33346781 No abstract available.
Diagnostic Modalities in Primary Immunodeficiency.
Raymond LS, Leiding J, Forbes-Satter LR. Raymond LS, et al. Clin Rev Allergy Immunol. 2022 Aug;63(1):90-98. doi: 10.1007/s12016-022-08933-1. Epub 2022 Mar 15. Clin Rev Allergy Immunol. 2022. PMID: 35290615 Review.
Cervical disc arthroplasty.
Zindrick M, Harris MB, Humphreys SC, O'Leary PT, Schneiderman G, Watters WC 3rd, Turkelson CM, Wies JL, Raymond L. Zindrick M, et al. Among authors: raymond l. J Am Acad Orthop Surg. 2010 Oct;18(10):631-7. doi: 10.5435/00124635-201010000-00006. J Am Acad Orthop Surg. 2010. PMID: 20889952 Review.
Diabetic firefighters.
Raymond LW, Guidotti TL, Rosenman KD. Raymond LW, et al. J Occup Environ Med. 2002 Jun;44(6):492-4; author reply 494. doi: 10.1097/00043764-200206000-00007. J Occup Environ Med. 2002. PMID: 12085473 No abstract available.
Biallelic variants in NSUN6 cause an autosomal recessive neurodevelopmental disorder.
Mattioli F, Worpenberg L, Li CT, Ibrahim N, Naz S, Sharif S, Firouzabadi SG, Vosoogh S, Saraeva-Lamri R, Raymond L, Trujillo C, Guex N, Antonarakis SE, Ansar M, Darvish H, Liu RJ, Roignant JY, Reymond A. Mattioli F, et al. Among authors: raymond l. Genet Med. 2023 Sep;25(9):100900. doi: 10.1016/j.gim.2023.100900. Epub 2023 May 21. Genet Med. 2023. PMID: 37226891 Free article.
560 results